TARGRETIN (bexarotene) by Bausch + Lomb. Approved for retinoid [epc]. First approved in 2000.
Drug data last refreshed 8h ago · AI intelligence enriched 1w ago
TARGRETIN (bexarotene) is a topical retinoid gel approved in 2000 for cutaneous T-cell lymphoma and other retinoid-responsive dermatologic conditions. It selectively binds retinoid X receptors (RXRs) to modulate gene expression and promote differentiation of malignant cells. The drug targets patients with mycosis fungoides and other rare skin lymphoproliferative disorders.
Product is approaching loss of exclusivity with modest competitive pressure (30/100), suggesting limited team expansion and focus on pipeline transition planning.
Retinoid
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Phase 3 Trial of Brentuximab Vedotin(SGN-35) Versus Physician's Choice (Methotrexate or Bexarotene) in Participants With CD30-Positive Cutaneous T-Cell Lymphoma (ALCANZA Study)
Phase I Study of CS-7017 and Bexarotene
Pralatrexate and Bexarotene in Patients With Relapsed or Refractory Cutaneous T-cell Lymphoma
Study Evaluating Two Dose Levels of Targretin Capsules in Participants With Refractory Cutaneous T-Cell Lymphoma (CTCL)
BATTLE Program: Tarceva and Targretin in Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
TARGRETIN offers limited career growth as a LOE-approaching product with minimal linked job openings and modest commercial spend. Roles on this product typically focus on defensive market management, customer retention, and supply-chain optimization rather than expansion or innovation.